Method to make ultra stable structural laminate

ABSTRACT

A method to make an ultra-stable structural laminate of a cementitious material with a nano-molecular veneer and a foam component catalytically reacted into an expanded closed cell foam having a thickness from ⅛ th  inch to 8 inches, a density from 1.5 pounds/cubic foot to 3 pounds/cubic foot that inter-engages the cementitious material forming a matrix creating the ultra-stable structural laminate with fire resistance; a lateral nail pull strength from 44 pounds to 300 pounds of force; an insulation R value from 1 to 40; a resistance to seismic impact for earthquakes over 3.1 on the Richter Scale; a break point from 7 lbs/inch to 100 lbs/inch; and a resistance to wind shear equivalent to a 15 mph downburst.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application claims priority to and the benefit of co-pendingU.S. Non Provisional patent application Ser. Nos. 16/006,554,16/006,570, 16/006,583 and 16/006,598 which claim priority to U.S.Provisional Patent Application Ser. No. 62/582,517 filed on Nov. 7,2017, entitled “PROCESS FOR MAKING A CEMENTITIOUS CONSTRUCTION MATERIAL”and U.S. Provisional Patent Application Ser. No. 62/582,545 filed onNov. 7, 2017, entitled “CEMENTITIOUS CONSTRUCTION MATERIAL”. All thesereferences are hereby incorporated in their entirety.

FIELD

The present embodiment generally relates to a method to make anultra-stable structural laminate with fire resistance and insulationproperties and an ability to resist seismic impact and wind shear.

BACKGROUND

A need exists for a method to make ultra-stable structural laminateswith fire resistance isolative properties, resistance to seismic impactand wind shear as well as resistance to mold, mildew, and termites.

The present embodiments meet these needs.

BRIEF DESCRIPTION OF THE DRAWINGS

The detailed description will be better understood in conjunction withthe accompanying drawings as follows:

FIG. 1A-1D depicts the stepwise process for making a cementitiousmaterial that can be deposited on the foam forming the ultra-stablestructural laminate.

FIG. 2 depicts the X-ray diffraction pre-treatment and post-treatment ofmagnesium oxychloride with phosphoric acid usable in creating thecementitious material usable on the closed cell foam of the ultra-stablestructural laminate.

FIG. 3A-3H depicts a table of cementitious material formulations made bythe method containing reinforcing components and aggregate and otheradditives along with physical properties of the formulations usable withthe expanded foam component of the ultra-stable structural laminate.

FIG. 4 is a table showing various additional cementitious materialformulations for use on the foam of the ultra-stable structural laminatewhich can be made by the inventive method.

The present embodiments are detailed below with reference to the listedFigures.

DETAILED DESCRIPTION OF THE EMBODIMENTS

Before explaining the method to make the ultra-stable structurallaminate in detail, it is to be understood that the ultra-stablestructural laminate is not limited to the particular embodiments andthat it can be practiced or carried out in various ways.

The invention relates to a method to make an ultra-stable structurallaminate with fire resistance; a lateral nail pull strength from 44 to300 pounds of force; an insulation R value from 1 to 40 and wherein theultra-stable structural laminate of a cementitious material with anano-molecular veneer is integrally reacted to a foam component that hasbeen catalytically reacted into an expanded closed cell foam having athickness from ⅛^(th) inch to 8 inches; a density from 1.5 pounds/cubicfoot to 3 pounds/cubic foot that self-engages to the cementitiousmaterial forming an ultra-stable structural laminate with fireresistance; a lateral nail pull strength from 44 pounds to 300 pounds offorce; an insulation R value from 1 to 40; a resistance to seismicimpact for earthquakes over 3.1 on the Richter Scale; a break point from7 lbs/inch to 100 lbs/inch; and a resistance to wind shear equivalent toa 15 mph downburst.

More specifically, the invention relates to a method to make acementitious material having 29 wt % to 40 wt % of a magnesium oxide drypowder containing 80 wt % to 98 wt % of magnesium oxide based on a finaltotal weight of the cementitious material, the magnesium oxide with asurface area ranging from 5 meters²/gram to 50 meters²/gram and anaverage particle size ranging from about 0.3 to about 90 microns whereinmore than about 90% by weight magnesium oxide particles are less than orequal to about 40 microns.

In addition, the method includes blending into the cementitious material14 wt % to 18 wt % of a magnesium chloride dissolved in water based onthe final total weight of the cementitious material.

The method includes blending into the cementitious material 0.1 wt % to10 wt % of a stabilizing material with a phosphorus-containing compoundbased on the final total weight of the cementitious material.

The stabilizing material with the phosphorus-containing compound can bea phosphorous acid (A) based on the final total weight of thecementitious material, wherein the phosphorous acid consists of anaqueous solution of 55 wt % to 65 wt % of a concentrate of H₃PO₃; or aphosphoric acid (B) based on the final total weight of the cementitiousmaterial, wherein the phosphoric acid consists of an aqueous solution of80 wt % to 90 wt % of a concentrate of H₃PO₄.

While implementing the method, a portion of the amorphous phasecementitious material grows a plurality of crystals, each crystal havinga MW within the range of 280 to 709, the amorphous phase cementitiousmaterial encapsulating the plurality of crystals, wherein a majority ofstabilizing material with a phosphorus-containing compound are consumedinto a nano-molecular veneer while increasing surface area of theplurality of crystals by 2% to 49% during curing.

The nano-molecular elements of the cured nano-molecular veneer areinsoluble in water and the cured nano-molecular veneer protects theplurality of crystals from degradation in water at temperatures from 20degrees to 60 degrees Celsius for from 24 hours to 56 days of the formedcementitious material.

The method to make the ultra-stable structural laminate includesutilizing a foam component that is catalytically reacted into anexpanded closed cell foam having a thickness from ⅛^(th) inch to 8inches and a density from 1.5 pounds/cubic foot to 3 pounds/cubic footthat reacts with the cementitious material in a manner akin toself-adherence, forming an ultra-stable structural laminate with fireresistance; a lateral nail pull strength from 44 to 300 pounds of force;an insulation R value from 1 to 40; a resistance to seismic impact forearthquakes over 3.1 on the Richter Scale; and a break point from 7 to100.

In embodiments, the method contemplates using as the expanded closedcell foam of the ultra-stable structural laminate, a pentane blownclosed cell polyurethane foam.

In embodiments, the method contemplates using as the ultra-stablestructural laminate foam component is at least one member of the group:a polyurethane, a polyisocyanurate, and a polystyrene.

The invention relates to a process wherein the ultra-stable cementitiousconstruction material consisting of a crystallized portion with anamorphous nano-molecular veneer substantially free of crystalline silicafor disposition on an expanded closed cell foam just after expanding.

The first step of the process for forming the cementitious constructionmaterial involves forming a gel phase by blending together magnesiumoxide and magnesium chloride in a water with a weight ratio of from1.9:1 to 2.1:1 of magnesium oxide to magnesium chloride.

In the process for forming the cementitious construction material, from2 weight percent to 30 weight percent of aggregate is added to the gelphase, forming an amorphous phase.

Phosphorous acid or phosphoric acid or both are then added to theamorphous phase, actuating crystallization of a portion of the amorphousphase, while simultaneously forming a nano-molecular veneerencapsulating the crystallized portion of the amorphous phase withoutdetectable magnesium phosphate and with from 2% to 49% increase insurface area as compared to veneer-free crystallized portions, andwherein the crystallized portion with nano-molecular veneer isconfigured to resist degradation in water having a temperature at 60degrees C. for 48 hours.

Benefits of the process for forming the cementitious constructionmaterial are as follows: increased cement stability when submerged inwater at temperatures up to 60 degrees C.; a physical property thatdetermines warm water stability for the above cement and no additionaltime required for this invention.

Benefits of the cementitious material formulation include increasedcement stability when submerged in water at temperatures up to 60degrees C. and improved racking for resistance to seismic events andwind sheer.

Benefits of the ultra-stable structural laminate is the integration ofthe cementitious material formulation with nano-molecular veneer intothe expanded closed cell foam just after expanding forming theultra-stable structural laminate, without degrading or losing thestructural advantages of the nano-molecular veneer and without the needfor nails or glue or epoxy, that may otherwise be required forconstruction materials.

The inventive process provides an ultra-stable structural laminate withincreased stability in environments with high temperatures and highmoisture.

The invention process involves creating an ultra-stable structurallaminate which has a cementitious material with a protective layer thatis not an exposed crystal, so that the laminate is not susceptible tomoisture or water dissolving at elevated temperatures.

The process creates an ultra-stable structural laminate that resistscorrosion in the presence of water.

This process creates an ultra-stable structural laminate with fireresistance and an improved water tolerance over other types of materialscontaining magnesium oxychloride cements without adding polymers orother sealants that can sacrifice some of the excellent fire-resistantproperties of magnesium oxychloride cements.

The process forms an ultra-stable structural laminate containing acementitious material with an unexpected amorphous layer that protectsthe magnesium oxychloride cement crystals is less detrimental to thestructural strength of the cement product than other uses of phosphoriccompounds have proven to be.

The first sequence of steps of the process for making the ultra-stablestructural laminate includes creating a cementitious materialformulation that first forms a gel phase by blending together magnesiumoxide and magnesium chloride in a water with a weight ratio of from1.9:1 to 2.1:1 of magnesium oxide to magnesium chloride.

In the process for making the ultra-stable structural laminate, thecementitious material is blended with from 2 weight percent to 30 weightpercent of aggregate while in the gel phase, forming an amorphous phase.

Phosphorous acid or phosphoric acid or both are then added to theamorphous phase, actuating crystallization of a portion of the amorphousphase, while simultaneously forming a nano-molecular veneerencapsulating the crystallized portion of the amorphous phase withoutdetectable magnesium phosphate and with a 2% to 49% increase in surfacearea as compared to veneer-free crystallized portions, and wherein thecrystallized portion with nano-molecular veneer is configured to resistdegradation in water having a temperature at 60 degrees C. for 48 hours.

Benefits of the process for making the cementitious material are asfollows: increased cement stability when submerged in water attemperatures up to 60 degrees C., a physical property that determineswarm water stability for the above cement, and no additional timerequired for this invention.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer includes adding 0.1 wt % to 30 wt %of an aggregate based on a final total weight of the concrete.

The aggregate can include particles having a diameter from 1 nm to 10mm, wherein the aggregate comprises at least one of: wood, perlite,styrene based foam beads, calcium carbonate powder, glass particulate,and combinations thereof.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can include adding: 0.1 wt % to 2 wt% of a reinforcing material based on a final total weight of thecementitious material, the reinforcing material comprising a non-wovenor woven silica containing mat, a non-woven or woven hydrocarboncontaining mat.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can includes: adding 0.1 weightpercent to 15 weight percent biomass added to the amorphous phasecementitious material based on the final total weight of the concrete.

The biomass can be a member of the group comprising: rice husks, cornhusks, and dung.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can include: adding 0.1 wt % to 10wt % of at least one surfactant to the cementitious material based onthe final total weight of the concrete to decrease porosity of aggregateand prevent amorphous phase cementitious material from entering pores ofthe aggregate.

The surfactant can be a detergent.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can include: adding 0.1 weightpercent to 5 weight percent of a re-dispersible powder polymer based onthe final total weight of the concrete.

The re-dispersible powder polymer is selected from the group consistingof silicon, polyurethane dispersion, polyurethane, alkyl carboxylic acidvinyl ester monomer, branched and unbranched alcohol(meth)acrylic acidester monomer, vinyl aromatic monomer, olefin monomer, diene monomer andvinyl halide monomer or a vinyl acetate ethylene “VAE”.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can include: adding 0.1 weightpercent to 5 weight percent based on the final total weight of thecementitious material of an acrylic or styrene butadiene rubber (SBR)into the concrete while the re-dispersible powder polymer is added.

In an embodiment, the process for making an ultra-stable cementitiousmaterial with nano-molecular veneer can include: adding 0.1 wt % to 15wt % of a reinforcing material based on the final total weight of theconcrete.

The reinforcing material can include at least one of: chopped silicacontaining fibers; hemp containing fibers; nano-molecular carbon fiberstrands; chopped carbon fibers; chopped hydrocarbon fiber; andcombinations thereof.

It should be noted that this unique laminate can be formed withoutrequiring weatherization prior to inspection of a nail patterns becauseonly finishing seams are required.

The process makes a unique laminate that is flame resistant which is asignificance advantage over known weatherizing building products.

The following definitions are used herein:

The term “aggregate” refers to a wood, perlite, foam beams, glass,calcium carbonate powder, or carbon fiber strands with a particle sizeno larger than 3 mm.

The term “amorphous phase” refers to a non-crystalline mixture of thefinal reacted products.

The term “amorphous nano-molecular veneer” refers to a coating bonded tothe crystallized portion that has a material which is not visible ascrystalline in an X-ray diffraction test, and has a density of moleculeswhich is inert to water molecules.

The term “biomass” refers to organic materials such as wood flour,straw, ground pecan shells, and ground up bagasse.

The term “cementitious construction material” refers to a board orstructure that is used for structural assembly to form facilities,offices, barns, homes, fences, and marine quarters for use on a ship oroil platform offshore.

The term “crystallized portion” refers to a segment of the createdcementitious construction material with activation energies of 70kilojoules per mole, having a monoclinic crystalline structure which inthis invention includes magnesium oxychloride.

The term “crystalline silica” refers to silica molecules, such as sand,in a crystalline phase, similar to glass.

The term “dispersible polymer” is a water dispersible ethylene-vinylacetate copolymer.

The term “encapsulating” refers to the creation of a nano-molecularveneer over surfaces of the crystals wherein the surface coating can beconnected, such as sandpaper which comprises many silica particlesadhered to a substrate with very little space between the silicaparticles. The dendritic nature of the plurality of crystals provide acoating that may be continuous or have small gaps.

The term “fibers” refers to needle-like materials that do not exceed 3mm in length, but could include longer fibers woven into a mat.

The term “gel phase” refers to a phase in which molecules attract toeach other without bonding in a slurry.

The term “insoluble in water” refers to a compound that will not go intosolution or degrade when exposed to water between ambient temperatureand 60 degrees C. for 0 hours to 48 hours.

The term “magnesium chloride in a water” refers to a liquid containinganhydrous magnesium chloride salt such as a water containing ananhydrous magnesium chloride salt with from 20 to 35 weight percent saltin the water which can be distilled water, dirty water containingparticulates and non-volatile organic matter, or clean tap water.

The term “magnesium oxide” refers to the powder form of MgO with from80% to 98% purity, the balance being calcium carbonate, quartz, or ironoxide or similar impurities naturally found in magnesite.

The term “magnesium phosphate crystals” refers to the crystals formed bythe reaction of magnesium oxide with phosphoric acid or phosphorousacid.

The term “nano-molecular elements” refers to the newly identified,insoluble in water, non-crystalline, phosphorous-containing species;identifiable with scan electron microscope (SEM) with elementalanalysis. This material will not show up as a phosphorous containingspecies on XRAY DIFFRACTION.

The term “phosphoric acid” refers to a concentrate of H₃PO₄ with adensity of 1.1 g/ml to 1.85 g/ml.

The term “phosphorous acid” refers a concentrate of H₃PO₃ with a densityof 1.1 g/ml to 1.65 g/ml.

The term “plurality of crystals” refers to the magnesium oxychloridecrystals which form from part of the amorphous phase.

The term “predetermined temperature for the water” refers to atemperature from ambient temperature to 90 degrees C.”

The term “preset period of time” refers to a window of time from 10hours to 90 hours, and specifically includes from 24 hours to 72 hours.

The phrase “protects the plurality of crystals from degradation inwater” refers to the nano-molecular veneer making the strength losslower than it would be without the nano-molecular veneer when thecementitious material is exposed to water between ambient temperatureand 60 degrees C. for 0-48 hours.

The term “substantially free” refers to a less than 3 weight percentcontent of crystalline silica based on x-ray diffraction testing in thecementitious construction material.

The term “surface area” refers to the surface area as tested using theBET theory methodology.

The term “veneer” refers to a chemically bonded protective layer on thecrystallized portion of the amorphous phase configured to resist waterwhich can be elevated to 60 degrees C. for extended periods of time.

The term “water” refers to H₂O with impurities of less than 0.5 weightpercent.

The aggregate includes particles based on a final total weight of thecementitious material, having a diameter from 1 nm to 10 mm.

The aggregate contains at least one of: wood, perlite, styrene basedfoam beads, calcium carbonate powder, glass particulate, andcombinations thereof.

The cementitious material with aggregate is blended to the amorphousphase with from 0.1 wt % to 2 wt % of a reinforcing material based on afinal total weight of the cementitious material.

The reinforcing material can be a non-woven or woven silica containingmat, a non-woven, or woven hydrocarbon containing mat.

In other embodiments, the reinforcing material can be chopped silicacontaining fibers; hemp containing fibers; nano-molecular carbon fiberstrands; chopped carbon fibers; chopped hydrocarbon fiber; andcombinations thereof.

The amorphous phase cementitious material containing aggregate can bepoured over the reinforcing material enabling a portion of the amorphousphase cementitious material to grow a plurality of crystals, eachcrystal having a MW within the range of 280 to 709, the amorphous phasecementitious material encapsulating the plurality of crystals.

A majority of stabilizing material with a phosphorus-containing compoundcan be consumed into a nano-molecular veneer while increasing surfacearea of the plurality of crystals by 2% to 49% during curing, andwherein the nano-molecular elements of the cured nano-molecular veneerare insoluble in water and the cured nano-molecular veneer protects theplurality of crystals from degradation in water at temperatures from 20degrees to 60 degrees Celsius for from 24 hours to 56 days of the formedcementitious material.

In embodiments of the cementitious material, 0.1 weight percent to 15weight percent biomass can be added to the amorphous phase cementitiousmaterial based on the final total weight of the cementitious material.

In embodiments of the cementitious material, 0.1 wt % to 10 wt % of atleast one surfactant is added to the cementitious material based on thefinal total weight of the cementitious material to decrease porosity ofaggregate and prevent amorphous phase cementitious material fromentering pores of the aggregate.

In embodiments of the cementitious material, 0.1 weight percent to 5weight percent of a re-dispersible powder polymer based on the finaltotal weight of the cementitious material can be incorporated in theamorphous phase cementitious material.

In embodiments of the cementitious material, the re-dispersible powderpolymer can be selected from the group consisting of acrylic, silicon,polyurethane dispersion, polyurethane, alkyl carboxylic acid vinyl estermonomer, branched and unbranched alcohol(meth)acrylic acid estermonomer, vinyl aromatic monomer, olefin monomer, diene monomer and vinylhalide monomer.

In embodiments of the cementitious material, 0.1 weight percent to 5weight percent based on the final total weight of the cementitiousmaterial of an acrylic or styrene butadiene rubber (SBR) can be blendedinto the amorphous cementitious material with the re-dispersible powderpolymer.

In embodiments of the cementitious material, 0.1 weight percent to 5weight percent based on the final total weight of the cementitiousmaterial of a re-dispersible polymer powder can be added to theamorphous cementitious material, wherein the re-dispersible polymerpowder is a member of the group consisting of: a vinyl ethylene esterand ethylene, a vinyl laurate vinyl chloride copolymer, a vinyl estermonomers, (meth)acrylate monomer, a vinyl aromatic monomer, an olefinmonomer, a 1,3-diene monomer, a vinyl halide monomer, a homopolymer orcopolymer derived from one or more monomers selected from the groupconsisting of a vinyl acetate, a vinyl ester of an alpha-branchedmonocarboxylic acids having from 9 to 11 carbon atoms, a vinyl chloride,an ethylene, a methyl acrylate, a methyl methacrylate, an ethylacrylate, an ethyl methacrylate, a propyl acrylate, a propylmethacrylate, an n-butyl acrylate, a n-butyl methacrylate, an2-ethylhexyl acrylate.

The invention relates to a building with an exterior building surfacecovered with the cementitious material of the formulations of theindependent claims of this application.

FIG. 1A shows the steps of the invention.

The process for making a cementitious construction material as step 100:forming a gel phase by blending together magnesium oxide and magnesiumchloride in water.

Step 110 can involve adding at least one of: a phosphorous acid and aphosphoric acid to the gel phase while forming an amorphous phase.

Step 120 can require adding from 2 weight percent to 30 weight percentof aggregate to the amorphous phase based on a total final weight of thecementitious construction material.

Step 130 can involve crystallizing a portion of the amorphous phase intoa plurality of crystals generating nano-molecular elements that projectfrom the plurality of crystals, encapsulating the plurality of crystals,forming a nano-molecular veneer without detectable magnesium phosphatecrystals while increasing surface area of the plurality of crystals by2% to 49%, and wherein the nano-molecular elements of the nano-molecularveneer are insoluble in water and the nano-molecular veneer protects theplurality of crystals from degradation in water at a predeterminedtemperature for a preset period of time.

In embodiments, the process for making a cementitious constructionmaterial can include adding from 0.1 weight percent to 15 weight percentbiomass to the gel phase based on the total final weight of thecementitious construction material.

In embodiments, the process for making a cementitious constructionmaterial can involve adding from 0.1 weight percent to 5 weight percentof a dispersible polymer to the gel phase based on the total finalweight of the cementitious construction material.

FIG. 1B shows a first embodiment incorporating the fewest steps neededto make the cementitious material.

Step 200 can include forming from 35 wt % to 79.9 wt % of a cementitiousmaterial based on the final total weight of the cementitious material.

Step 201 can involve blending from 29 wt % to 40 wt % of a magnesiumoxide dry powder containing 80 wt % to 98 wt % of magnesium oxide basedon a final total weight of the cementitious material into 14 wt % to 18wt % of a magnesium chloride dissolved in water based on a final totalweight of the cementitious material.

Step 202 can involve mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water forming a liquid suspension whileminimizing adding gas into the liquid suspension.

Step 204 can involve adding from 0.1 wt % to 10 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

Step 206 can involve reacting during a preset unit of time, the mixedliquid suspension into an amorphous phase cementitious material.

Step 208 can involve blending to the amorphous phase cementitiousmaterial from 0.1 wt % to 30 wt % of an aggregate comprising particlesbased on a final total weight of the tile backer board, having adiameter from 1 nm to 10 mm, wherein the aggregate comprises at leastone of: wood, perlite, styrene based foam beads, calcium carbonatepowder, glass particulate, and combinations thereof.

Step 210 can involve pouring the flowable concrete over from 0.1 wt % to2 wt % of a reinforcing material based on a final total weight of thetile backer board forming a reinforced concrete.

Step 212 can involve forming during a preset unit of time, in a portionof the amorphous phase cementitious material a plurality of crystals ofa defined Molecular Weight from the amorphous non-crystallinenano-molecular cementitious material encapsulating the plurality ofcrystals, creating a nano-molecular veneer without detectablephosphorus-containing compound while increasing surface area of theplurality of crystals.

Step 213 can involve catalytically reacting a foam component into anexpanded closed cell foam having a thickness from ⅛^(th) inch to 8inches and a density from 1.5 pounds/cubic foot to 3 pounds/cubic footthat self-adheres to the cementitious material forming an ultra-stablestructural laminate with fire resistance and a lateral nail pullstrength from 44 to 300 pounds of force, an insulation R value from 1 to40, a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale, a break point from 7 to 100 lbs/inch; and a resistance towind shear equivalent to a 15 mph downburst.

FIG. 1C depicts additional steps to be used with the embodiment of FIG.1A to make the cementitious material.

FIG. 1C depicts:

Step 220 can include adding from 0.1 wt % to 15 wt % biomass to theamorphous phase cementitious material based on the final total weight ofthe cementitious material.

Step 222 can include adding from 0.1 wt % to 10 wt % of at least onesurfactant which is added to the cementitious material based on thefinal total weight of the cementitious material to decrease porosity ofaggregate and prevent amorphous phase cementitious material fromentering pores of the aggregate.

Step 224 can include adding from 0.1 weight percent to 5 weight percentof a re-dispersible powder polymer based on the final total weight ofthe cementitious material into the amorphous phase cementitiousmaterial.

Step 226 can include blending from 0.1 weight percent to 5 weightpercent of an acrylic or styrene butadiene rubber (SBR) based on thefinal total weight of the cementitious material into the amorphouscementitious material with the re-dispersible powder polymer.

FIG. 1D shows steps of another embodiment to make the cementitiousmaterial forming a tile baker board.

Step 250 can include forming from 55 wt % to 99.8 wt % of a cementitiousmaterial based on the final total weight of the tile backer board.

Step 252 can include forming from 55 wt % to 99.8 wt % of a cementitiousmaterial by blending 29 wt % to 40 wt % of a magnesium oxide dry powdercontaining from 80 wt % to 98 wt % of magnesium oxide based on a finaltotal weight of the based on the cementitious material with from 14 wt %of 18 wt % of a magnesium chloride dissolved in water based on based onthe final total weight of the tile backer board, to form a liquidsuspension.

Step 254 can involve adding from 0.1 wt % to 10 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the tile backer board to the liquid suspension.

Step 256 can include allowing the liquid suspension to react into anamorphous phase cementitious material during a preset period of time.

Step 258 can involve adding from 0.1 wt % to 30 wt % of an aggregatebased on the total weight of the tile backer board to the amorphousphase cementitious material.

Step 260 can involve adding from 0.1 wt % to 15 wt % of a reinforcingmaterial based on the final total weight of the tile backer board, tothe amorphous phase cementitious material, wherein the reinforcingmaterial is at least one of: chopped silica containing fibers; hempcontaining fibers; nano-molecular carbon fiber strands; chopped carbonfibers; chopped hydrocarbon fiber; and combinations thereof.

Step 262 can involve growing a portion of the amorphous phasecementitious material grows a plurality of crystals, each crystal havinga MW within the range of 283 to 709, the amorphous phase cementitiousmaterial encapsulating the plurality of crystals, wherein a majority ofstabilizing material with a phosphorus-containing compound are consumedinto a nano-molecular veneer while increasing surface area of theplurality of crystals by 2% to 49% during curing, and wherein thenano-molecular elements of the cured nano-molecular veneer are insolublein water and the cured nano-molecular veneer protects the plurality ofcrystals from degradation in water at temperatures from 20 degrees to 60degrees Celsius for from 24 hours to 56 days of the formed tile backerboard.

Step 263 involves catalytically reacting a foam component into anexpanded closed cell foam having a thickness from ⅛^(th) inch to 8inches and a density from 1.5 pounds/cubic foot to 3 pounds/cubic footthat self-adheres to the cementitious material forming an ultra-stablestructural laminate with fire resistance and a lateral nail pullstrength from 44 to 300 pounds of force, an insulation R value from 1 to40, a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale, a break point from 7 to 100 lbs/inch; and a resistance towind shear equivalent to a 15 mph downburst.

In embodiments, the cementitious construction material can create anano-molecular veneer with a thickness from 1 microns to 3 microns.

In embodiments, the cementitious construction material can be used tocreate a cementitious construction material configured to support a loadof at least 2.5 pounds per square foot.

In embodiments, the cementitious construction material produces productcan be used to create a home, an office, a warehouse, a shed, a dock,artwork, aqueducts, or another load supporting structure.

In embodiments, the water is a brine or similar salt solution with aconcentration of 2% to 30% salt.

In embodiments, the cementitious construction material can containfibers.

In variations of the cementitious construction material, prior tocrystallizing the amorphous phase, an additional substrate can beintroduced and coated with the cementitious construction material havingoriented strand board, plywood, waterproof membrane, concrete, and wood,and coated with the amorphous phase increasing fire resistance andstability in hot water.

The cementitious construction material can include at least onesurfactant added to the amorphous phase to decrease porosity ofaggregates and prevent amorphous phase from entering pores of theaggregates.

The surfactants can be any molecule that reduces the surface porosity ofthe aggregates being used in the cement.

In embodiments, the amorphous phase can be crystallized using atemperature from 40 to 50 degrees C. for a period of time from 3 to 24hours, at a relative humidity from 30 to 100 percent.

In embodiments, the cementitious construction material can be formedusing an exothermic reaction, such as generating 10 to 15 degrees ofheat for the duration of the reaction.

In embodiments, the cementitious construction material gel phase can beformed using intimate mixing for at least 3 minutes prior to addingaggregate.

FIG. 2 shows diffractograms of cured samples produced from X-raydiffraction at 28 degrees C. The major 5 phase peaks are labelled. Thefour upper quadrants are post phosphoric acid treatment and the bottomquadrant is pre phosphoric acid treatment.

The importance of this FIG. 2 is the area under the peaks.

Example 1

A ultra-stable structural laminate is formed with a cementitiousmaterial formed by blending 29 wt % to 40 wt % of a magnesium oxide drypowder containing 80 wt % to 98 wt % of magnesium oxide based on a finaltotal weight of the cementitious material, with 14 wt % to 18 wt % of amagnesium chloride dissolved in water and reacting to form a liquidsuspension, mixing from 2 to 10 minutes, adding a phosphorus-containingmaterial, and allowing the liquid suspension to react into an amorphousphase cementitious material, wherein a portion of the amorphous phasecementitious material grows a plurality of crystals forming anano-molecular veneer.

After forming the cementitious material, a foam component iscatalytically reacted into an expanded closed cell foam having athickness from ⅛^(th) inch to 8 inches and a density from 1.5pounds/cubic foot to 3 pounds/cubic foot that reacts with thecementitious material similar to self-adhering to the cementitiousmaterial forming an ultra-stable structural laminate with fireresistance; a lateral nail pull strength from 44 to 300 pounds of force;an insulation R value from 1 to 40; a resistance to seismic impact forearthquakes over 3.1 on the Richter Scale; a break point from 7 to 100lbs/inch; and a resistance to wind shear equivalent to a 15 mphdownburst.

The cementitious material made by the steps of this example has a 78%crystallized portion with 12% of an amorphous nano-molecular veneersubstantially free of crystalline silica.

To create the cementitious material, first a gel phase is formed byblending together magnesium oxide powder with a purity of 85% by weightand a magnesium chloride in a brine with density of 1.26.

The magnesium oxide is blended in a weight ratio of 2:1 with themagnesium chloride based on the total final weight of the cementitiousconstruction material.

Next, from 20 weight percent of aggregate from wood is added to the gelphase forming the amorphous phase.

To the amorphous phase, 5 weight percent of phosphoric acid is addedbased on the total final weight of the cementitious constructionmaterial.

To complete forming of the cementitious material, 65% of the amorphousphase is crystallized by extruding the amorphous phase between twolayers of fiberglass on a carrier sheet. The sandwich-like material iscured at 45 to 55 degrees Centigrade for 12 to 24 hours at a relativehumidity greater than 55% creating a board with a thickness of 12 mm.

A nano-molecular veneer is formed over the crystallized portion with aveneer thickness of 1 micron encapsulating the portion of thecrystallized portion without producing detectable magnesium phosphate.The nano-molecular veneer has a 30% increase in surface area as comparedto veneer-free crystallized portions.

The final crystallized portion with nano-molecular veneer is configuredto resist degradation in water having a temperature at 60 degrees C. for48 hours.

In this example, the foam component is polyurethane and the foamcomponent is expanded catalytically into an expanded closed cell foamhaving a specific thickness of ⅛^(th) inch and a specific density of 1.5pounds/cubic foot that self-adheres to the cementitious material formingan ultra-stable structural laminate with fire resistance and a lateralnail pull strength of 40 pounds of force, an insulation R value of 1, aresistance to seismic impact for earthquakes over 3.1 on the RichterScale, a break point of 7 lbs/inch; and a resistance to wind shearequivalent to a 15 mph downburst.

Example 2

The novel cementitious material is formed by first combining 34 wt % ofa magnesium oxide dry powder containing 85 wt % purity of magnesiumoxide based on a final total weight of the cementitious material.

The magnesium oxide used has a surface area ranging from 5 meters²/gramto 50 meters²/gram and an average particle size ranging from about 0.3to about 90 microns wherein more than about 90% by weight magnesiumoxide particles are less than or equal to about 40 microns.

16 wt % of a magnesium chloride was dissolved in water based on a finaltotal weight of the cementitious material. The magnesium chloride inaqueous solution was: 29 wt % of a magnesium chloride aqueous solution.The magnesium oxide and the magnesium chloride in water reacted to forma liquid suspension.

1.3 wt % of a stabilizing material with a phosphorus-containing compoundbased on a final total weight of the cementitious material was thenmixed with the liquid suspension and the mixture reacted into anamorphous phase cementitious material.

The stabilizing material with the phosphorus-containing compound wasphosphoric acid (B) based on the final total weight of the cementitiousmaterial, wherein the phosphoric acid consisted of an aqueous solutionof 85 wt % of a concentrate of H₃PO₄. The mixture reacted into anamorphous phase cementitious material.

The amorphous phase cementitious material grows a plurality of crystals,each crystal having a MW of 530 generating nano-molecular elements thatproject from the plurality of crystals, encapsulating the plurality ofcrystals, wherein a majority of stabilizing material with aphosphorus-containing compound are consumed into the non-molecularveneer while increasing surface area of the plurality of crystals by49%, and wherein the nano-molecular elements of the nano-molecularveneer are insoluble in water and the nano-molecular veneer protects theplurality of crystals from degradation in water at 60 degrees Celsiusfor 24 hours forming the cementitious material.

In this example, the foam component is a polyisocyanurate, wherein thepolyisocyanurate is catalytically expanded into an expanded closed cellfoam having a thickness of 3 inches, a density of 2 pounds/cubic footthat reacts to intimately engage, much like self-adhering, to thecementitious material forming an ultra-stable structural laminate withfire resistance; a lateral nail pull strength of 100 pounds of force; aninsulation R value of 12; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 15 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

Example 3

In this example, the process creates anultra-stable structural laminatethat includes a cementitious material with 35 wt % of a magnesium oxidedry powder containing 80 wt % purity of magnesium oxide based on a finaltotal weight of the cementitious material.

The magnesium oxide used has a surface area ranging from 5 meters²/gramto 50 meters²/gram and an average particle size ranging from about 0.3to about 90 microns wherein more than about 90% by weight magnesiumoxide particles are less than or equal to about 40 microns.

15 wt % of a magnesium chloride dissolved in water based on a finaltotal weight of the cementitious material was mixed with the magnesiumoxide,

In this example, the magnesium chloride in aqueous solution was a 27 wt% a magnesium chloride aqueous solution. The magnesium oxide and themagnesium chloride in water were mixed and react to form a liquidsuspension.

2.5 wt % of a stabilizing material with a phosphorus-containing compoundbased on a final total weight of the cementitious material was mixedwith the liquid suspension, the mixture reacted into an amorphous phasecementitious material, the stabilizing material with thephosphorus-containing compound contained a phosphorous acid (A) based onthe final total weight of the cementitious material. The phosphorousacid consisted of an aqueous solution of 60 wt % of a concentrate ofH₃PO₃.

A portion of the amorphous phase cementitious material grew a pluralityof crystals, developed with each crystal having a MW of 283, 413, 530,or 709, generating nano-molecular elements that projected from theplurality of crystals, encapsulating the plurality of crystals.

A majority of phosphorous-containing compounds from the stabilizingmaterial with a phosphorus-containing compound were consumed into thenon-molecular veneer while increasing surface area of the plurality ofcrystals by 2% to 49%.

The nano-molecular elements of the nano-molecular veneer were insolublein water and the nano-molecular veneer protected the plurality ofcrystals from degradation in water at 60 degrees Celsius for 24 hours asthe cementitious material.

In this example, the foam component is polystyrene and the polystyreneis expanded, such as with a catalyst, into an expanded closed cell foamhaving a thickness of 2 inches and a density of 2.5 pounds/cubic footthat intimately engages, such as by self-adherance, to the cementitiousmaterial forming an ultra-stable structural laminate with fireresistance; a lateral nail pull strength of 80 pounds of force; aninsulation R value of 12; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 12 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

FIGS. 3A-3H show many samples of the formulation of the cementitiousmaterial and their associated physical properties which are integratedwithout the use of glues or epoxies or nails into an expanded closedcell foam which are prepared according to the inventive method.

Sample 1 of the ultra-stable structural laminate contains a cementitiousmaterial with 29 wt % of a magnesium oxide dry powder based on a finaltotal weight of the cementitious material was used. The magnesium oxidedry powder containing 85 wt % purity of magnesium oxide.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 14 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 1, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 0.1 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 1, the stabilizing material with the phosphorus-containingcompound was a phosphorous acid based on the final total weight of thecementitious material, wherein the phosphorous acid consists of anaqueous solution of 60 wt % of a concentrate of H₃PO₃.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

The flowable, uncured cementitious material was then poured on a mold tocure and form a cement.

For this Sample 1, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 2% to 20 m²/g.

The cured material of Sample 1 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent that is a polyurethane and the polyurethane is expanded intoan expanded closed cell foam having a thickness of 2 inches and adensity of 1.7 pounds/cubic foot that self-adheres to the cementitiousmaterial forming an ultra-stable structural laminate with fireresistance; a lateral nail pull strength of 120 pounds of force; aninsulation R value of 12; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 40 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

Sample 2

Sample 2 of the ultra-stable structural laminate contains a cementitiousmaterial with 40 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the of thecementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 18 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 2, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 10 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 2, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

The flowable, uncured cementitious material was then poured on a moldand cured, forming a cement.

For this Sample 2, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 49% to 29 m²/g.

The cured material of Sample 2 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent of polyurethane that was catalytically expanded into anexpanded closed cell foam having a thickness of 1 inch and a density of1.7 pounds/cubic foot that self-adheres to the cementitious material asthe cementitious material cures forming an ultra-stable structurallaminate with fire resistance; a lateral nail pull strength of 96 poundsof force; an insulation R value of 8; a resistance to seismic impact forearthquakes over 3.1 on the Richter Scale; a break point of 23 lbs/inch;and a resistance to wind shear equivalent to a 15 mph downburst.

Sample 3

Sample 3 of the ultra-stable structural laminate contains a cementitiousmaterial with 32 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the of thecementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 17 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 3, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 0.1 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of cementitious material the mixed liquid suspension.

For Sample 3, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

The reinforcing component was a non-woven silica-containing mat. Thereinforcing component was 0.1 wt % based on the total final weight ofthe cementitious material.

For this Sample 3, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 2% to 20 m²/g.

The cured material of Sample 3 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent of a polyurethane that is expanded into an expanded closedcell foam having a thickness of 1.5 inches and a density of 3pounds/cubic foot that self-adheres to the cementitious material formingan ultra-stable structural laminate with fire resistance; a lateral nailpull strength of 110 pounds of force; an insulation R value of 11; aresistance to seismic impact for earthquakes over 3.1 on the RichterScale; a break point of 29 lbs/inch; and a resistance to wind shearequivalent to a 15 mph downburst.

Sample 4

Sample 4 of the ultra-stable structural laminate contains a cementitiousmaterial with 31 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the of thecementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 16 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 4, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 1 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 4, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

The reinforcing component was 2 wt % chopped silica fibers based on thetotal final weight of the cementitious material.

For this Sample 4, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 23% to 24 m²/g.

The cured material of Sample 4 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded into anexpanded closed cell foam having a thickness of 2.5 inches and a densityof 1.7 pounds/cubic foot that self-adheres to the cementitious materialforming an ultra-stable structural laminate with fire resistance; alateral nail pull strength of 139 pounds of force; an insulation R valueof 16; a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale; a break point of 44 lbs/inch; and a resistance to windshear equivalent to a 15 mph downburst.

Sample 5

Sample 5 of the ultra-stable structural laminate has a cementationsmaterial that contains 32.5 wt % of a magnesium oxide dry powdercontaining 85 wt % of magnesium oxide based on a final total weight ofthe cementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 17.5 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 5, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 1.75 wt % of astabilizing material with a phosphorus-containing compound based on afinal total weight of the cementitious material to the mixed liquidsuspension.

For Sample 5, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 5 contains 0.1 wt % of aggregate component known aswood:perlite:styrene based foam beads in a 30:8:1 ratio based on thetotal final weight of the cementitious material was added into theamorphous phase cementitious material forming a flowable concrete.

The flowable, uncured concrete was then poured on a mold and cured tomake a finished concrete. The expanded closed cell foam was disposedover the concrete and the two reacted to form the ultra-stablestructural laminate.

For this Sample 5, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by more than 38% to27 m²/g.

The cured material of Sample 5 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC. Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded into anexpanded closed cell foam having a thickness of 8 inches and a densityof 3 pounds/cubic foot that self-adheres to the cementitious materialforming an ultra-stable structural laminate with fire resistance; alateral nail pull strength of 300 pounds of force; an insulation R valueof 40; a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale; a break point of 100 lbs/inch; and a resistance to windshear equivalent to a 15 mph downburst.

Sample 6

Sample 6 of the ultra-stable structural laminate contains a cementitiousmaterial with 33 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the cementitiousmaterial was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 18 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 6, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 2.5 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material the mixed liquid suspension.

For Sample 6, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 6 contains 30 wt % of aggregate component of wood:perlite:styrenebased foam beads in a 30:8:1 ratio based on the total final weight ofthe cementitious material was added into the amorphous phasecementitious material forming a flowable concrete.

The flowable, uncured concrete was then poured into a mold and cured tomake a finished concrete.

For this Sample 6, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by more than 49% to29 m²/g.

The cured material of Sample 6 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded into anexpanded closed cell foam using a catalyst to have a thickness of 3inches and a density of 2 pounds/cubic foot that self-adheres to thecementitious material forming an ultra-stable structural laminate withfire resistance; a lateral nail pull strength of 166 pounds of force; aninsulation R value of 19; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 51 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

Sample 7

Sample 7 of the ultra-stable structural laminate contains a cementitiousmaterial with 33 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the cementitiousmaterial was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 19 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 7, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 3.75 wt % of astabilizing material with a phosphorus-containing compound based on afinal total weight of the cementitious material to the mixed liquidsuspension.

For Sample 7, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 7 contains a biomass of 0.1 weight percent based on the totalfinal weight of the cementitious material. The biomass of this examplewas rice husks.

For this Sample 7, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 49% to 29 m²/g.

The cured material of Sample 7 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded into anexpanded closed cell foam having a thickness of 3.5 inches and a densityof 1.7 pounds/cubic foot that self-adheres to the cementitious materialforming an ultra-stable structural laminate with fire resistance; alateral nail pull strength of 170 pounds of force; an insulation R valueof 22; a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale; a break point of 56 lbs/inch; and a resistance to windshear equivalent to a 15 mph downburst.

Sample 8

Sample 8 of the ultra-stable structural laminate contains a cementitiousmaterial of 32 wt % of a magnesium oxide dry powder containing 85 wt %of magnesium oxide based on a final total weight of the cementitiousmaterial was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 17 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 7, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 5 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 8, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 8 contains 15 wt % of biomass based on the total final weight ofthe cementitious material was added into the amorphous phasecementitious material forming a flowable concrete. The biomass was cornhusks.

The flowable, uncured concrete was then poured into a mold, the finishedmaterial forming a concrete.

For this Sample 8, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by more than 44% to28 m²/g.

The cured material of Sample 8 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded into anexpanded closed cell foam having a thickness of 4 inches and a densityof 1.7 pounds/cubic foot that self-adheres to the cementitious materialforming an ultra-stable structural laminate with fire resistance; alateral nail pull strength of 185 pounds of force; an insulation R valueof 25; a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale; a break point of 61 lbs/inch; and a resistance to windshear equivalent to a 15 mph downburst.

Sample 9

Sample 9 of the ultra-stable structural laminate has a cementitiousmaterial that contains 35 wt % of a magnesium oxide dry powdercontaining 85 wt % of magnesium oxide based on a final total weight ofthe cementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 16 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 9, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 6.25 wt % of astabilizing material with a phosphorus-containing compound based on afinal total weight of the cementitious material to the mixed liquidsuspension.

For Sample 9, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

0.1 weight percent of a surfactant, namely a detergent was added to theamorphous phase cementitious material based on the final total weight ofthe cementitious material.

The flowable, uncured concrete was then poured into a mold forming afinished concrete.

For this Sample 9, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 23% to 24 m²/g.

The cured material of Sample 9 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent that is a polyurethane and the polyurethane is expanded intoan expanded closed cell foam using catalyst until the polyurethane has athickness of 4.5 inches and a density of 1.7 pounds/cubic foot thatself-adheres to the cementitious material forming an ultra-stablestructural laminate with fire resistance; a lateral nail pull strengthof 200 pounds of force; an insulation R value of 28; a resistance toseismic impact for earthquakes over 3.1 on the Richter Scale; a breakpoint of 67 lbs/inch; and a resistance to wind shear equivalent to a 15mph downburst.

Sample 10

Sample 10 of the ultra-stable structural laminate contains acementitious material with 30 wt % of a magnesium oxide dry powdercontaining 85 wt % of magnesium oxide based on a final total weight ofthe cementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 18 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 10, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 7.5 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 10, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 10 contains 10 wt % of sodium stearate as a surfactant, based onthe total final weight of the cementitious material was added into theamorphous phase cementitious material forming a flowable concrete.

The flowable, uncured concrete was then poured in a mold forming afinished concrete.

For this Sample 10, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by more than 38% to27 m²/g.

The cured material of Sample 10 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is expanded using acatalyst into an expanded closed cell foam having a thickness of 5inches and a density of 2.1 pounds/cubic foot that self-adheres to thecementitious material forming an ultra-stable structural laminate withfire resistance; a lateral nail pull strength of 215 pounds of force; aninsulation R value of 31; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 73 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

Sample 11

Sample 11 of the ultra-stable structural laminate contains acementitious material with 33 wt % of a magnesium oxide dry powdercontaining 85 wt % of magnesium oxide based on a final total weight ofthe cementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 15 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 11, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 8.75 wt % of astabilizing material with a phosphorus-containing compound based on afinal total weight of the cementitious material to the mixed liquidsuspension.

For Sample 11, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

0.1 weight percent of re-dispersible polymer, namely vinyl acetateethylene (VAE) was added to the amorphous phase cementitious materialbased on the final total weight of the cementitious material.

The flowable, uncured concrete was then poured into a mold forming afinished concrete.

For this Sample 11, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by more than 49% to29 m²/g.

The cured material of Sample 11 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent of polyurethane and the polyurethane is expanded into anexpanded closed cell foam having a thickness of 0.5 inches and a densityof 1.6 pounds/cubic foot that self-adheres to the cementitious materialforming an ultra-stable structural laminate with fire resistance and alateral nail pull strength 108 pounds of force, an insulation R value of4, a resistance to seismic impact for earthquakes over 3.1 on theRichter Scale, a break point from 22 lbs/inch; and a resistance to windshear equivalent to a 15 mph downburst.

Sample 12

Sample 12 of the ultra-stable structural laminate contains acementitious material with contains 32 wt % of a magnesium oxide drypowder containing 85 wt % of magnesium oxide based on a final totalweight of the cementitious material was used.

The magnesium oxide had a surface area ranging from 5 meters²/gram to 50meters²/gram and an average particle size ranging from about 0.3 toabout 90 microns wherein more than about 90% by weight magnesium oxideparticles were less than or equal to about 40 microns.

The magnesium oxide was blended with 19 wt % of a magnesium chloridedissolved in water based on a final total weight of the cementitiousmaterial.

For Sample 12, the magnesium chloride in aqueous solution was a 28 wt %magnesium chloride aqueous solution.

After 3 minutes of mixing with a planetary mixer, the magnesium oxideand the magnesium chloride in water form a liquid suspension whileminimizing adding gas into the liquid suspension.

For this sample, the next step involved adding 10 wt % of a stabilizingmaterial with a phosphorus-containing compound based on a final totalweight of the cementitious material to the mixed liquid suspension.

For Sample 12, the stabilizing material with the phosphorus-containingcompound was a phosphoric acid based on the final total weight of thecementitious material, wherein the phosphoric acid consists of anaqueous solution of 80 wt % to 90 wt % of a concentrate of H₃PO₄.

The liquid suspension with stabilizing material was permitted to reactinto an amorphous phase cementitious material for a period of time of 2minutes.

Sample 12 contains 5 wt % of vinyl acetate ethylene based on the totalfinal weight of the cementitious material was added into the amorphousphase cementitious material forming a flowable concrete.

The flowable, uncured concrete was then poured into a mold formingfinished concrete.

For this Sample 12, a portion of the amorphous phase cementitiousmaterial formed a plurality of crystals, each crystal is known as a“Magnesium Oxychloride Cement Crystals” having a MW of 530.7 withamorphous non-crystalline nano-molecular cementitious materialencapsulating the plurality of crystals, creating a nano-molecularveneer without detectable phosphorus-containing compound whileincreasing surface area of the plurality of crystals by 49% to 29 m²/g.

The cured material of Sample 12 formed a cementitious material which asstable in water at 60 degrees Celsius for 24 hours using the JetProducts, LLC Warm Water Stability Test as authenticated by ClemsonUniversity Chemical Engineering Department in 2017.

In this example, the cementitious material is disposed over a foamcomponent is a polyurethane and the polyurethane is catalyticallyexpanded into an expanded closed cell foam having a thickness of 0.75inches and a density of 1.8 pounds/cubic foot that self-adheres to thecementitious material forming an ultra-stable structural laminate withfire resistance; a lateral nail pull strength of 82 pounds of force; aninsulation R value of 5; a resistance to seismic impact for earthquakesover 3.1 on the Richter Scale; a break point of 23 lbs/inch; and aresistance to wind shear equivalent to a 15 mph downburst.

What is claimed is:
 1. A method to make an ultra-stable structurallaminate with fire resistance; a lateral nail pull strength from 44 to300 pounds of force and an insulation R value from 1 to 40, the methodcomprising: (i) Forming a cementitious material with a nano-molecularveneer by combining: (a) 29 wt % to 40 wt % of a magnesium oxide drypowder containing 80 wt % to 98 wt % of magnesium oxide based on a finaltotal weight of the cementitious material, the magnesium oxide with asurface area ranging from 5 meters²/gram to 50 meters²/gram and anaverage particle size ranging from about 0.3 to about 90 microns whereinmore than about 90% by weight magnesium oxide particles are less than orequal to about 40 microns; (b) 14 wt % to 18 wt % of a magnesiumchloride dissolved in water based on the final total weight of thecementitious material; (c) 0.1 wt % to 10 wt % of a stabilizing materialwith a phosphorus-containing compound based on the final total weight ofthe cementitious material, the stabilizing material with thephosphorus-containing compound comprising: a. a phosphorous acid (A)based on the final total weight of the cementitious material, whereinthe phosphorous acid consists of an aqueous solution of 55 wt % to 65 wt% of a concentrate of H₃PO₃; or b. a phosphoric acid (B) based on thefinal total weight of the cementitious material, wherein the phosphoricacid consists of an aqueous solution of 80 wt % to 90 wt % of aconcentrate of H₃PO₄; growing a plurality of crystals in a portion ofthe amorphous phase cementitious material, each crystal having a MWwithin the range of 280 to 709, the amorphous phase cementitiousmaterial encapsulating the plurality of crystals, wherein a majority ofstabilizing material with a phosphorus-containing compound are consumedinto a nano-molecular veneer while increasing surface area of theplurality of crystals by 2% to 49% during curing, and wherein thenano-molecular elements of the cured nano-molecular veneer are insolublein water and the cured nano-molecular veneer protects the plurality ofcrystals from degradation in water at temperatures from 20 degrees to 60degrees Celsius for from 24 hours to 56 days of the formed cementitiousmaterial; and (ii) catalytically reacting a foam component into anexpanded closed cell foam having a thickness from ⅛^(th) inch to 8inches, a density from 1.5 pounds/cubic foot to 3 pounds/cubic foot;(iii) disposing to intimately inter-engage the cementitious materialover the expanded closed cell foam as a matrix while expanding formingan ultra-stable structural laminate with fire resistance; a lateral nailpull strength from 44 pounds to 300 pounds of force; an insulation Rvalue from 1 to 40; a resistance to seismic impact for earthquakes over3.1 on the Richter Scale; a break point from 7 lbs/inch to 100 lbs/inch;and a resistance to wind shear equivalent to a 15 mph downburst.
 2. Themethod to make the ultra-stable structural laminate of claim 1,comprising adding 0.1 wt % to 30 wt % of an aggregate based on a finaltotal weight of the concrete, the aggregate comprising particles, havinga diameter from 1 nm to 10 mm, wherein the aggregate comprises at leastone of: wood, perlite, styrene based foam beads, calcium carbonatepowder, glass particulate, and combinations thereof.
 3. The method tomake the ultra-stable structural laminate of claim 2 comprising addingto the cementitious material 0.1 wt % to 2 wt % of a reinforcingmaterial based on the final total weight of the cementitious material,the reinforcing material comprising a non-woven or woven silicacontaining mat, a non-woven or woven hydrocarbon containing mat.
 4. Themethod to make the ultra-stable structural laminate of claim 1,comprising adding to the cementitious material 0.1 weight percent to 15weight percent biomass added to the amorphous phase cementitiousmaterial based on the final total weight of the concrete and mixing from3 to 10 minutes.
 5. The method to make the ultra-stable structurallaminate of claim 4, wherein the biomass is a member of the groupcomprising: rice husks, corn husks, and dung.
 6. The method to make theultra-stable structural laminate of claim 2, comprising adding to thecementitious material: 0.1 wt % to 10 wt % of at least one surfactant tothe cementitious material based on the final total weight of theconcrete to decrease porosity of aggregate and prevent amorphous phasecementitious material from entering pores of the aggregate.
 7. Themethod to make the ultra-stable structural laminate of claim 6, whereinthe surfactant is a detergent.
 8. The method to make the ultra-stablestructural laminate of claim 2, comprising adding to the cementitiousmaterial 0.1 weight percent to 5 weight percent of a re-dispersiblepowder polymer based on the final total weight of the concrete andmixing from 3 to 10 minutes.
 9. The method to make the ultra-stablestructural laminate of claim 8, wherein the re-dispersible powderpolymer is selected from the group consisting of: silicon, polyurethanedispersion, polyurethane, alkyl carboxylic acid vinyl ester monomer,branched and unbranched alcohol(meth)acrylic acid ester monomer, vinylaromatic monomer, olefin monomer, diene monomer and vinyl halide monomeror a vinyl acetate ethylene “VAE”.
 10. The method to make theultra-stable structural laminate of claim 8, further comprising addingto the cementitious material 0.1 weight percent to 5 weight percentbased on the final total weight of the cementitious material of anacrylic or styrene butadiene rubber (SBR) into the concrete while there-dispersible powder polymer is added.
 11. The method to make theultra-stable structural laminate of claim 1, wherein the expanded closedcell foam is a pentane blown closed cell polyurethane foam.
 12. Themethod to make the ultra-stable structural laminae of claim 1, whereinthe foam component is at least one member of the group: a polyurethane,a polyisocyanurate and a polystyrene.
 13. The method to make theultra-stable structural laminate of claim 1, further comprising addingto the cementitious material: 0.1 wt % to 15 wt % of a reinforcingmaterial based on the final total weight of the concrete, thereinforcing material comprising at least one of: (i) chopped silicacontaining fibers; (ii) hemp containing fibers; (iii) nano-molecularcarbon fiber strands; (iv) chopped carbon fibers; (v) choppedhydrocarbon fibers; and combinations thereof.